Canonical Allele Identifier: PA095505
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 167133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Glu414Lys
CA234086
NM_000159.4:c.1240G>A